Herbal extracts differentially inhibit oxidative effects caused by the biotransformation of nifurtimox, nitrofurantoin and acetaminophen on rat liver microsomes
Author
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Letelier, María E.
Author
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Iturra Montecinos, Pablo
Author
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Gallardo Garrido, Carlos
Admission date
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2018-12-20T15:13:18Z
Available date
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2018-12-20T15:13:18Z
Publication date
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2017
Cita de ítem
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Boletin Latinoamericano y del Caribe de Plantas Medicinales y Aromaticas, Volumen 16, Issue 2, 2017, Pages 88-98
Identifier
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07177917
Identifier
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https://repositorio.uchile.cl/handle/2250/158580
Abstract
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Inflammation is a cellular defensive mechanism associated to oxidative stress. The administration of nitrofurantoin, nifurtimox and acetaminophen generates oxidative stress by their biotransformation through CYP450 system. The main adverse effect described for the first two drugs is gastrointestinal inflammation and that of the last, hepatitis. Therefore, standardised dry extracts from Rosmarinus officinalis, Buddleja globosa Hope, Cynara scolymus L., Echinacea purpurea and Hedera helix were tested to evaluate their capacity to decrease drug-induced oxidative stress. For that, rat liver microsomes were incubated with drugs in the presence of NADPH (specific CYP450 system cofactor) to test oxidative damage on microsomal lipids, thiols, and GST activity. All drugs tested induced oxidation of micro somal lipids and thiols, and inhibition of GST activity. Herbal extracts prevented these phenomena in different extension. These results show that antioxidant phytodrugs previously evaluated could alleviate drugs adverse effects associated to oxidative stress.
Boletin Latinoamericano y del Caribe de Plantas Medicinales y Aromaticas
Keywords
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Antioxidants
Keywords
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GST
Keywords
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Herbal extracts
Keywords
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Herbal thiols
Keywords
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Oxidation inhibition
Keywords
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Polyphenols
Título
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Herbal extracts differentially inhibit oxidative effects caused by the biotransformation of nifurtimox, nitrofurantoin and acetaminophen on rat liver microsomes
Title in another language
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Extractos herbales inhiben diferencialmente los efectos oxidativos causados por la biotransformación nifurtimox, nitrofurantoína y acetaminofeno en microsomas hepáticos de rata